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H-Glu-Tyr-OH

PubChem CID: 515717

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Compound Synonyms H-Glu-Tyr-OH, 3422-39-7, Glu-Tyr, L-Glutamyl-L-Tyrosine, glutamyltyrosine, EY dipeptide, glutamyl-tyrosine, alpha-Glu-Tyr, E-Y Dipeptide, MFCD00063199, alpha-L-Glu-L-Tyr, L-Glu-L-Tyr, L-Glutamyl-L-Tyrosin, Glutamate Tyrosine dipeptide, Glutamate-Tyrosine dipeptide, L-alpha-glutamyl-L-tyrosine, SCHEMBL159463, CHEBI:73513, DTXSID90326069, EY, HY-P4595, DA-53975, FG108041, L-Tyrosine, L-.alpha.-glutamyl-, monomer, CS-0655365, Q27140594, (4S)-4-amino-5-[[(1S)-1-carboxy-2-(4-hydroxyphenyl)ethyl]amino]-5-oxopentanoic acid, Melanin synthesized from Glu-Tyr substrate catalyzed by tyrosinase for 40 hrs, (4S)-4-amino-5-[[(1S)-2-hydroxy-1-[(4-hydroxyphenyl)methyl]-2-oxo-ethyl]amino]-5-oxo-pentanoic acid, E-Y
Topological Polar Surface Area 150.0
Hydrogen Bond Donor Count 5.0
Heavy Atom Count 22.0
Description Glutamyltyrosine, also known as alpha-glu-tyr or E-Y, is a member of the class of compounds known as dipeptides. Dipeptides are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. Glutamyltyrosine is practically insoluble (in water) and a weakly acidic compound (based on its pKa). Glutamyltyrosine can be found in soy bean, which makes glutamyltyrosine a potential biomarker for the consumption of this food product. Glutamyltyrosine can be found primarily in feces.
Isotope Atom Count 0.0
Molecular Complexity 406.0
Database Name fooddb_chem_all;hmdb_chem_all;pubchem
Defined Atom Stereocenter Count 2.0
Iupac Name (4S)-4-amino-5-[[(1S)-1-carboxy-2-(4-hydroxyphenyl)ethyl]amino]-5-oxopentanoic acid
Nih Violation False
Class Carboxylic acids and derivatives
Xlogp -3.8
Superclass Organic acids and derivatives
Is Pains False
Subclass Amino acids, peptides, and analogues
Molecular Formula C14H18N2O6
Inchi Key YSWHPLCDIMUKFE-QWRGUYRKSA-N
Rotatable Bond Count 8.0
State Solid
Synonyms alpha-Glu-tyr, alpha-Glutamyltyrosine, alpha-L-Glu-L-tyr, E-Y, EY, L-Glu-L-tyr, a-Glu-tyr, Α-glu-tyr, a-Glutamyltyrosine, Α-glutamyltyrosine, a-L-Glu-L-tyr, Α-L-glu-L-tyr, Α-L-glutamyl-L-tyrosine, L-Α-glutamyl-L-tyrosine, N-Α-glutamyltyrosine, N-Α-L-glutamyl-L-tyrosine, N-L-Α-glutamyltyrosine, N-L-Α-glutamyl-L-tyrosine, alpha-L-Glutamyl-L-tyrosine, L-alpha-Glutamyl-L-tyrosine, N-alpha-Glutamyltyrosine, N-alpha-L-Glutamyl-L-tyrosine, N-L-alpha-Glutamyltyrosine, N-L-alpha-Glutamyl-L-tyrosine, NSC 523821, Glu-tyr, L-Glutamyl-L-tyrosine, N-Glutamyltyrosine, N-L-Glutamyl-L-tyrosine, Glutamyl-tyrosine, Glutamic acid tyrosine dipeptide, Glutamate tyrosine dipeptide, Glutamic acid-tyrosine dipeptide, Glutamate-tyrosine dipeptide, e-Y dipeptide, EY dipeptide, Glutamyltyrosine
Compound Name H-Glu-Tyr-OH
Kingdom Organic compounds
Exact Mass 310.116
Formal Charge 0.0
Brenk Violation False
Monoisotopic Mass 310.116
Hydrogen Bond Acceptor Count 7.0
Molecular Weight 310.3
Covalent Unit Count 1.0
Total Atom Stereocenter Count 2.0
Total Bond Stereocenter Count 0.0
Molecular Framework Aromatic homomonocyclic compounds
Inchi InChI=1S/C14H18N2O6/c15-10(5-6-12(18)19)13(20)16-11(14(21)22)7-8-1-3-9(17)4-2-8/h1-4,10-11,17H,5-7,15H2,(H,16,20)(H,18,19)(H,21,22)/t10-,11-/m0/s1
Smiles C1=CC(=CC=C1C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)O)N)O
Defined Bond Stereocenter Count 0.0
Taxonomy Direct Parent Dipeptides

  • 1. Outgoing r'ship FOUND_IN to/from Glycine Max (Plant) Rel Props:Source_db:fooddb_chem_all